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The Effect of Mycophenolate Mofetil on Non-Renal Manifestations in Systemic Lupus Erythematosus: Results from Korean Lupus Network Registry

Jung UH, Kwak SG, Choe JY, Lee SS, Kim SK

BACKGROUND: The objective of this study was to identify the effects of mycophenolate mofetil (MMF) on non-renal manifestations in systemic lupus erythematosus (SLE). METHODS: The study population comprised 439 SLE patients...
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Endoscopic Findings of Children with Familial Mediterranean Fever

Sağ E, Demir F, Saygın I, Kalyoncu M, Çakır M

PURPOSE: Familial Mediterranean fever (FMF) is an auto inflammatory disease characterized by periodic fever, synovitis and serositis. Patients may be admitted to gastroenterology units due to gastrointestinal symptoms. In this...
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Familial Mediterranean fever presenting as fever of unknown origin in Korea

Lee JH, Kim JH, Shim JO, Lee KC, Lee JW, Lee JH, Chae JJ

Familial Mediterranean fever (FMF) is the most common Mendelian autoinflammatory disease, characterized by uncontrolled activation of the innate immune system that manifests as recurrent brief fever and polyserositis (e.g., peritonitis,...
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Familial Mediterranean Fever With Complete Symptomatic Remission During Pregnancy

Kim KT, Jang HJ, Lee JE, Kim MK, Yoo JJ, Lee GY, Kae SH, Lee J

Familial Mediterranean fever (FMF) is an inherited autosomal recessive disorder, ethnically restricted and commonly found among populations surrounding the Mediterranean Sea. FMF is the most prevalent autoinflammatory disease; is characterized...
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A Case of Intravascular Large B-cell Lymphoma Mimicking Systemic Lupus Erythematosus

Park CK, Lee JC, Kang SW, Shim SC, Yun HJ, Kim JM, Yoo IS

Intravascular large B-cell lymphoma (IVLBCL) is a rare subtype of non-Hodgkin's lymphoma (NHL) and that progresses rapidly and is usually fatal. Because it usually presents with nonspecific symptoms, such as...
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Systemic Lupus Erythematosus with Initial Presentation of Ascites

Chu JM, Kang SH, Song JH, Han KH, Shin SY, Yang TY, Choi JJ, Hong SP

Systemic lupus erythematosus (SLE) is a chronic inflammatory disease of unknown etiology and is characterized by presence of variable pathogenic auto-antibodies and multiple organ involvement. Serositis is common in SLE,...
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An Unusual Case of Severe Neonatal Lupus Mimicking Neonatal Sepsis and Literature Review

Park HM, Jun HG, Park JH, Choi SW, Oh KW, Oh JS

Neonatal lupus is an uncommon autoimmune disease that results from transplacental passage of the maternal anti-SSA/Ro and/or anti-SSB/La antibodies. Pancytopenia or severe jaundice is a rare manifestation of neonatal lupus,...
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Autoinflammatory Diseases

Lee SH

Autoinflammatory diseases (AIDs) refer to a broad range of genetically mediated conditions characterized by recurrent attacks of systemic inflammation with typical manifestations of fever, rash, serositis, lymphadenopathy, and musculoskeletal symptoms....
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A Case of Rheumatoid Pneumoconiosis Presenting with Pleuritis and Pericarditis

Park MS, Kang DG, Jung EJ, Oh KJ, Sim JS, Kim EJ, Kim C

Caplan's syndrome is characterized by multiple small distinct nodules with progressive massive fibrosis and rheumatic arthritis in pneumoconiosis. Although pleural effusions occur infrequently as an extra-articular manifestation, pleuritis can develop...
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Pathogenesis and clinical manifestations of juvenile rheumatoid arthritis

Hahn YS, Kim JG

Juvenile rheumatoid arthritis (JRA) is the most common rheumatic childhood disease; its onset is before 16 years of age and it persists for at least 6 weeks. JRA encompasses a...
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Adult Onset Still's Disesae: A Case Report

Kim BJ, Kim SY, Kim GM

  • KMID: 2301955
  • Korean J Dermatol.
  • 2009 Oct;47(10):1203-1205.
Adult-onset Still's disease (AOSD) is a systemic inflammatory disease of an unknown etiology, and AOSD is characterized by high fever, skin rash, arthritis, lymphadenopathy, hepatomegaly, sore throat and serositis. The...
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The technique and the safety of laparoscopic incidental appendectomy using single loop during gynecologic laparoscopic surgery

Kim JJ, Kim DH, Lee SH, Park MY, Lee MK, Kim JY, Chung RJ

  • KMID: 2273181
  • Korean J Obstet Gynecol.
  • 2007 Sep;50(9):1254-1259.
OBJECTIVE: To introduce the technique of laparoscopic incidental appendectomy using single loop during gynecologic laparoscopic surgery and to demonstrate the safety of it. METHODS: This was a retrospective case-controlled study of...
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Adult Onset Still's Disease

Lee DH, Park JW, Hyun JW, Kim DH, Suh YS

  • KMID: 2294530
  • J Korean Acad Fam Med.
  • 2007 Mar;28(3):210-213.
Adult onset Still's disease (AOSD) is an uncommon acute systemic inflammatory disease of unknown origin. The clinical features include high spiking fever, arthralgia or arthritis, transient maculopapular rash, lymphadenopathy, hepatosplenomegaly,...
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A Case of Successful Treatments of Venous Leg Ulcers in Secondary Antiphospholipid Syndrome

Kim BK, Choi ST, Son MK, Lee KH, Lee SW, Chung SJ, Gil JH, Park YB, Lee SK

Antiphospholipid syndrome is an autoimmune disorder characterized by recurrent arterial or venous thrombosis, and pregnancy loss. A 57-year-old woman was admitted for aggravation of both leg ulcers. Venogram showed chronic...
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A Case of Cytophagic Histiocytic Panniculitis Involving the Extrapleural Fat

Seo JK, Choi JH, Lee SM, Lee SK

  • KMID: 2302244
  • Korean J Dermatol.
  • 2007 Feb;45(2):180-184.
Cytophagic histiocytic panniculitis gap (CHP) was described in 1980 as a chronic histiocytic disease of the subcutaneous tissue and associated with systemic manifestations such as fever, serositis, and hepatosplenomegaly. The...
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A Case of Adult-Onset Still's Disease Presented with Urticaria

Hong KK, Lew BL, Yang YI, Kim NI

  • KMID: 2302356
  • Korean J Dermatol.
  • 2006 Jan;44(1):63-66.
Adult-onset Still's diseas e(AOSD) is a rare, systemic inflammatory disease of unknown etiology, characterized by spiking fever, skin rash, arthralgia or arthritis, lymphadenopathy, hepatosplenomegaly, sore throat and serositis. The typical...
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A Case of Adult-onset Still's Disease associated with Congestive Heart Failure

Park BH, Min JY, Yeo CD, Oh SS, Hur KH, Hur SE, Kim JS, Kim WC, Kim WU

  • KMID: 2334819
  • J Korean Rheum Assoc.
  • 2005 Sep;12(3):235-239.
Adult onset Still's disease (AOSD) is a multi-systemic inflammatory disorder characterized by several distinguished manifestations including high spiking fever, evanescent salmon-colored skin rash, arthralgia/arthritis, hepato-splenomegaly, lymphadenopathy, sore throat, serositis, and...
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A Case of Erythema Nodosum and Serositis Associated with Myelodysplastic Syndrome

Choi JH, Ahn MJ, Park YW, Oh HS, Lee YY, Kim IS

Myelodysplastic syndrome (MDS) is a heterogenous group of stem cell disorders usually characterized by progressive refractory cytopenias, which could progress to acute myeloid leukemia. MDS may be associated with a...
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A case of systemic lupus erythematosus presented with refractory serositis and nephritis during pregnancy

Park HR, Song JS, Shin JI, Park BH, Park W

  • KMID: 1927332
  • Korean J Med.
  • 2004 Nov;67(Suppl 3):S896-S901.
Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by autoantibodies and immune complex depositions, has been known that it could be aggravated during pregnancy. We report a case who...
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A Case of recurrent adult onset still's disease with interstitial pneumonitis

Ryoo ES, Moon SH, Bae SB, Kim SG, Lee GG, Hong GY, Lee TY, Kim JS, Kim HT

  • KMID: 2251371
  • Korean J Med.
  • 1999 Aug;57(2):220-224.
Adult onset Still's disease(AOSD) is characterized by a high spiking fever, a transient rash, and arthritis. The clinical features include lymphadenopathy, hepatospleno-megaly, serositis, and sore throat. Leukocytosis is generally marked,...
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